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Advances in Protein Chemistry and Structural Biology|January 13, 2019
Structural and functional insights on the roles of molecular chaperones in the mistargeting and aggregation phenotypes associated with primary hyperoxaluria type IJosé Ángel Fernández-Higuero, Isabel Betancor-Fernández, Noel Mesa-Torres, et al.
Frontiers in Molecular Biosciences|December 12, 2022
Effect of naturally-occurring mutations on the stability and function of cancer-associated NQO1: Comparison of experiments and computationJuan Luis Pacheco-Garcia, Matteo Cagiada, Kelly Tienne-Matos, et al.
Plos One|November 9, 2013
The role of protein denaturation energetics and molecular chaperones in the aggregation and mistargeting of mutants causing primary hyperoxaluria type INoel Mesa-Torres, Israel Fabelo-Rosa, Debora Riverol, et al.
Plos One|August 15, 2014
Domain organization, catalysis and regulation of eukaryotic cystathionine beta-synthasesTomas Majtan, Angel L Pey, Roberto Fernández, et al.
The Journal of Biological Chemistry|June 1, 2007
Structure of phenylalanine hydroxylase from Colwellia psychrerythraea 34H, a monomeric cold active enzyme with local flexibility around the active site and high overall stabilityHanna-Kirsti S Leiros, Angel L Pey, Marte Innselset, et al.
The Journal of Clinical Investigation|July 4, 2008
Identification of pharmacological chaperones as potential therapeutic agents to treat phenylketonuriaAngel L Pey, Ming Ying, Nunilo Cremades, et al.
International Journal of Biological Macromolecules|January 1, 2021
Intrinsically disordered protein NUPR1 binds to the armadillo-repeat domain of Plakophilin 1Patricia Santofimia-Castaño, Bruno Rizzuti, Angel L Pey, et al.
Biochemistry|May 23, 2012
Conformational properties of nine purified cystathionine β-synthase mutantsAleš Hnízda, Tomas Majtan, Lu Liu, et al.
Handbook of Experimental Pharmacology|November 10, 2017
Potential Pharmacological Chaperones for Cystathionine Beta-Synthase-Deficient HomocystinuriaTomas Majtan, Angel L Pey, Paula Gimenez-Mascarell, et al.
Human Molecular Genetics|March 24, 2016
Molecular basis of classic galactosemia from the structure of human galactose 1-phosphate uridylyltransferaseThomas J McCorvie, Jolanta Kopec, Angel L Pey, et al.
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